FDA inspection

SmithKline Beecham Pharma GmbH & co. KG: FDA inspection ending Jun 27, 2017

FDA inspection 1019795 · Voluntary Action Indicated (VAI) · Dresden

Key facts

Inspection ID 1019795
Firm SmithKline Beecham Pharma GmbH & co. KG
FEI number 3004835618
Address Zirkusstr. 40
City Dresden
Country Germany
Fiscal year 2017
Inspection end date Jun 27, 2017
Classification Voluntary Action Indicated (VAI)
Project area Vaccines and Allergenic Products
Product type Biologics

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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